Odorono Liquid
NDC Package 51048-201-25

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Odorono (aluminum chlorohydrate) liquids is Use: Reduces underarm wetness. This formulation utilizes a liquid delivery system. Marketed by Omega & Delta Co, this product is identified by NDC 51048-201 and is authorized under FDA application M019.

Identification & Billing

NDC Package Code
51048-201-25
Package Description
74 mL in 1 BOTTLE, WITH APPLICATOR
Product Code
11-Digit Billing Format
51048020125

Clinical Specifications

Proprietary Name
Odorono Antiperspirant And Deodorant Roll-on Original
Non-Proprietary Name
Aluminum Chlorohydrate
Substance Name
Aluminum Chlorohydrate
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Usage Information
Use: Reduces underarm wetness

Regulatory & Marketing

Labeler Name
Omega & Delta Co
Product Type
Human Otc Drug
FDA Application #
M019
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-08-2006
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 51048-201-25 identifies a specific commercial package of 74 ml in 1 bottle, with applicator of Odorono Antiperspirant And Deodorant Roll-on Original, a human over the counter drug labeled by Omega & Delta Co. This liquid is formulated for topical use and contains aluminum chlorohydrate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Omega & Delta Co on May 08, 2006. The current certification is valid through December 31, 2027.

How is this Omega & Delta Co product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51048020125. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
51048-201-25
11-Digit CMS (5-4-2)
51048-0201-25

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.